Literature DB >> 22129223

Diversity-oriented approach to macrocyclic cyclophane derivatives by Suzuki-Miyaura cross-coupling and olefin metathesis as key steps.

Sambasivarao Kotha1, Arjun S Chavan, Mobin Shaikh.   

Abstract

Palladium-catalyzed Suzuki-Miyaura (SM) cross-coupling reaction with allylboronic acid pinacol ester and titanium assisted cross-metathesis (CM)/ring-closing metathesis (RCM) cascade has been used to synthesize macrocyclic cyclophane derivatives.

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Year:  2011        PMID： 22129223     DOI： 10.1021/jo2020714

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  5 in total

Review 1.  Selected synthetic strategies to cyclophanes.

Authors:  Mukesh Eknath Shirbhate; Gopalkrushna T Waghule; Sambasivarao Kotha
Journal:  Beilstein J Org Chem       Date:  2015-07-29       Impact factor: 2.883

2.  Hybrid macrocycle formation and spiro annulation on cis-syn-cis-tricyclo[6.3.0.0(2,6)]undeca-3,11-dione and its congeners via ring-closing metathesis.

Authors:  Sambasivarao Kotha; Ajay Kumar Chinnam; Rashid Ali
Journal:  Beilstein J Org Chem       Date:  2015-07-06       Impact factor: 2.883

3.  Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps.

Authors:  Ajay Kumar Chinnam; Mukesh Eknathrao Shirbhate; Sambasivarao Kotha
Journal:  Beilstein J Org Chem       Date:  2015-08-31       Impact factor: 2.883

Review 4.  Quinone and hydroquinone metabolites from the ascidians of the genus Aplidium.

Authors:  Camila Spereta Bertanha; Ana Helena Januário; Tavane Aparecida Alvarenga; Letícia Pereira Pimenta; Márcio Luis Andrade E Silva; Wilson Roberto Cunha; Patrícia Mendonça Pauletti
Journal:  Mar Drugs       Date:  2014-06-12       Impact factor: 5.118

Review 5.  Synergistic approach to polycycles through Suzuki-Miyaura cross coupling and metathesis as key steps.

Authors:  Sambasivarao Kotha; Milind Meshram; Chandravathi Chakkapalli
Journal:  Beilstein J Org Chem       Date:  2018-09-21       Impact factor: 2.883
  5 in total

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